Package 0781-5223-01

Brand: carvedilol

Generic: carvedilol
NDC Package

Package Facts

Identity

Package NDC 0781-5223-01
Digits Only 0781522301
Product NDC 0781-5223
Product ID 0781-5223_56b48372-0a73-4242-a65c-2b65abdb70c5
Description

100 TABLET, FILM COATED in 1 BOTTLE (0781-5223-01)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand carvedilol
Generic carvedilol
Sample Package No

Linked Drug Pages (1)

Carvedilol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56b48372-0a73-4242-a65c-2b65abdb70c5", "openfda": {"nui": ["N0000000099", "N0000009923", "N0000009924", "N0000175553", "N0000175556"], "unii": ["0K47UL67F2"], "rxcui": ["200031", "200032", "200033", "686924"], "spl_set_id": ["da8b8c20-0130-4aa9-924d-4a4f28c3f767"], "pharm_class_epc": ["alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-5223-01)", "package_ndc": "0781-5223-01", "marketing_end_date": "20260831", "marketing_start_date": "20070905"}], "brand_name": "Carvedilol", "product_id": "0781-5223_56b48372-0a73-4242-a65c-2b65abdb70c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "Adrenergic beta1-Antagonists [MoA]", "Adrenergic beta2-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0781-5223", "generic_name": "Carvedilol", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carvedilol", "active_ingredients": [{"name": "CARVEDILOL", "strength": "12.5 mg/1"}], "application_number": "ANDA078227", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20070905"}